96-10-6 Usage
Description
DIETHYLALUMINUM CHLORIDE is a colorless liquid that is highly reactive and poses a significant fire and explosion hazard. It is primarily used as an intermediate in the production of organometallic compounds.
Used in Chemical Industry:
DIETHYLALUMINUM CHLORIDE is used as a catalyst and reagent in various chemical reactions, including the synthesis of organometallic compounds, olefin polymerization, and hydroalumination reactions. Its high reactivity and ability to form strong bonds with other elements make it a valuable component in the production of various chemicals and materials.
Used in Petrochemical Industry:
In the petrochemical industry, DIETHYLALUMINUM CHLORIDE is used as a catalyst in the production of polymers and plastics. Its ability to initiate and control polymerization reactions allows for the creation of materials with specific properties and characteristics, making it an essential component in the synthesis of various polymers.
Used in Pharmaceutical Industry:
DIETHYLALUMINUM CHLORIDE is also used in the pharmaceutical industry as an intermediate in the synthesis of various drugs and pharmaceutical compounds. Its reactivity and ability to form stable bonds with other molecules make it a useful component in the development of new drugs and therapies.
Used in Research and Development:
Due to its unique properties and reactivity, DIETHYLALUMINUM CHLORIDE is often used in research and development settings to explore new chemical reactions and syntheses. Its ability to form stable bonds with a wide range of elements makes it a valuable tool for scientists and researchers working to develop new materials and compounds.
Air & Water Reactions
Pyrophoric in air [Hawley]. Reacts violently with water, Rose(1961).
Reactivity Profile
Organometallics, such as DIETHYLALUMINUM CHLORIDE, are reactive with many other groups. Incompatible with acids and bases. Organometallics are good reducing agents and therefore incompatible with oxidizing agents. Often reactive with water to generate toxic or flammable gases. Organometallics containing halogens (fluorine, chlorine, bromine, iodine) bonded to the metal typically with generate gaseous hydrohalic acids (HF, HCl, HBr, HI) with water.
Purification Methods
Distil it from excess dry NaCl (to remove ethyl aluminium dichloride) in a 50-cm column containing a heated nichrome spiral. [Beilstein 4 IV 4403.]
Check Digit Verification of cas no
The CAS Registry Mumber 96-10-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96-10:
(4*9)+(3*6)+(2*1)+(1*0)=56
56 % 10 = 6
So 96-10-6 is a valid CAS Registry Number.
InChI:InChI=1/2C2H5.Al.ClH/c2*1-2;;/h2*1H2,2H3;;1H/q;;+1;/p-1/rC4H10Al.ClH/c1-3-5-4-2;/h3-4H2,1-2H3;1H/q+1;/p-1
96-10-6Relevant articles and documents
METHOD FOR MANUFACTURING DIALKYL ZINC AND DIALKYL ALUMINUM MONOHALIDE
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Page/Page column 8, (2011/02/25)
Disclosed is a manufacturing method for dialkyl zinc and dialkyl aluminum monohalide that makes it possible to efficiently manufacture both dialkyl zinc and dialkyl aluminum monohalide of high purity and at a high yield on an industrial scale with a single reaction from zinc chloride and trialkyl aluminum starting materials, while suppressing the production of precipitates in the reaction process and suppressing the adhesion of precipitates to the equipment and the admixture thereof into the product. The manufacturing method for dialkyl zinc and dialkyl aluminum monohalide is a dialkyl zinc and dialkyl aluminum monohalide manufacturing method that causes a reaction between zinc chloride and trialkyl aluminum, and uses trialkyl aluminum with a hydride concentration of 0.01 mass% to 0.10 mass%. Dialkyl zinc that contains essentially no aluminum is separated from the reactants, and then dialkyl aluminum monohalide that contains essentially no zinc is separated.
Effect of crystallization water and nature of an aluminum alkyl on the reduction of Eu3+ to Eu2+ in interaction of EuCl 3 ? 6H2O with Bu 3 i Al and Et3Al
Bulgakov,Kuleshov,Makhmutov
, p. 1342 - 1345 (2010/01/05)
Volumetric and photoluminescence analytical techniques were employed to study the effect of crystallization water and nature of an aluminum alkyl on the reduction of Eu3+ to Eu2+ in a heterophase interaction of EuCl3 ? 6H
Stereoselective olefin polymerization catalysts generated by the transfer-epimetalation of olefins or acetylenes with dialkyltitanium(IV) complexes: Three-membered metallocycles as proposed chiral sites
Eisch, John J.,Gitua, John N.
, p. 4172 - 4174 (2008/10/08)
Efficient transfer-epimetalations of simple olefins and acetylenes by R2TiL2 reagents (R = Bun, But; L = X) are readily achieved in THF at -78°C to generate titanacyclopropa(e)ne intermediates, readily capable o